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As a Senior Quality Engineer, you will lead the verification and validation of medical device systems, develop compliance documentation, manage risk assessments, and provide guidance in Computer System Validation, ensuring adherence to FDA regulations and industry standards. You'll engage in collaborative efforts, supporting quality assurance processes and training team members.

As a Software Engineer on the Tempus Next Cardio team, you will develop and release AI-enabled software aimed at identifying patients with gaps in clinical care. You will collaborate with cross-disciplinary teams to create performant and maintainable software solutions, utilizing a modern tech stack.

The Senior Manager, Quality Engineering is responsible for overseeing postmarket surveillance activities, ensuring compliance with FDA and ISO regulations, managing complaint handling processes, and collaborating with cross-functional teams for product lifecycle management and quality assurance. This role involves creating procedures for monitoring product safety and effectiveness, leading investigations into complaints, and providing training and guidance on regulatory processes.